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一种用于普通狨猴的稳健微珠阻塞性青光眼模型。

A Robust Microbead Occlusion Model of Glaucoma for the Common Marmoset.

机构信息

Department of Biological and Vision Sciences, State University of New York College of Optometry, New York, NY, USA.

出版信息

Transl Vis Sci Technol. 2022 Jan 3;11(1):14. doi: 10.1167/tvst.11.1.14.

Abstract

PURPOSE

To establish a robust experimental model of glaucoma in the common marmoset (Callithrix jacchus), a New World primate, using an intracameral microbead injection technique.

METHODS

Elevated intraocular pressure (IOP) was induced by an injection of polystyrene microbeads. Morphologic changes in the retina and optic nerve of glaucomatous eyes were assessed and electroretinogram (ERG) recordings were performed to evaluate functional changes.

RESULTS

Microbead injections induced a sustained IOP elevation for at least 10 weeks in a reproducible manner. At the end of the 10-week experimental period, there was significant loss of retinal ganglion cells (RGCs) in all quadrants and eccentricities, although it was more prominent in the mid-peripheral and peripheral regions. This was consistent with a thinning of the Retinal nerve fiber layer (RNFL) seen in spectral domain optical coherence tomography scans. Surviving RGCs showed marked changes in morphology, including somatic shrinkage and dendritic atrophy. Retinas also showed significant gliosis. The amplitude of the ERG photopic negative response, with subsequent a- and b-wave changes, was reduced in glaucomatous eyes. The optic nerve of glaucomatous eyes showed expanded cupping, disorganization of the astrocytic matrix, axonal loss, and gliosis.

CONCLUSIONS

We developed a robust and reproducible model of glaucoma in the marmoset. The model exhibits both structural and functional alterations of retina and optic nerve characteristic of glaucoma in humans and animal models.

TRANSLATIONAL RELEVANCE

The glaucoma model in the marmoset described here forms a robust method to study the disease etiology, progression, and potential therapies in a nonhuman primate, allowing for more effective translation of animal data to humans.

摘要

目的

建立一种新的世界灵长类动物——普通狨猴(Callithrix jacchus)的青光眼实验模型,使用房内微珠注射技术。

方法

通过注射聚苯乙烯微珠来升高眼内压(IOP)。评估青光眼眼视网膜和视神经的形态变化,并进行视网膜电图(ERG)记录以评估功能变化。

结果

微珠注射以可重复的方式在至少 10 周内引起持续的 IOP 升高。在 10 周的实验期末,所有象限和偏心度的视网膜神经节细胞(RGC)都有明显的丢失,尽管在中周和周边区域更为明显。这与光谱域光学相干断层扫描中所见的视网膜神经纤维层(RNFL)变薄一致。存活的 RGC 表现出明显的形态变化,包括体细胞缩小和树突萎缩。视网膜也表现出明显的神经胶质增生。青光眼眼中的 ERG 明视负反应的振幅降低,随后 a 波和 b 波发生变化。青光眼眼中的视神经显示杯状扩大、星形胶质细胞基质紊乱、轴突丢失和神经胶质增生。

结论

我们在狨猴中建立了一种可靠且可重复的青光眼模型。该模型表现出与人以及动物模型中的青光眼相似的视网膜和视神经的结构和功能改变。

翻译

骆仪

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c9e/8762714/6c1b7a7a8284/tvst-11-1-14-f001.jpg

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